Does CENOBAMATE Cause Product dose omission in error? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product dose omission in error have been filed in association with CENOBAMATE (Xcopri). This represents 0.2% of all adverse event reports for CENOBAMATE.
11
Reports of Product dose omission in error with CENOBAMATE
0.2%
of all CENOBAMATE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission in error From CENOBAMATE?
Of the 11 reports, 1 (9.1%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CENOBAMATE. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does CENOBAMATE Cause?
Seizure (1,544)
Product dose omission issue (1,229)
Fatigue (608)
Somnolence (588)
Dizziness (486)
Off label use (376)
Product use issue (364)
Fall (323)
Headache (301)
Wrong technique in product usage process (268)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which CENOBAMATE Alternatives Have Lower Product dose omission in error Risk?
CENOBAMATE vs CEPHALEXIN
CENOBAMATE vs CERITINIB
CENOBAMATE vs CERLIPONASE ALFA
CENOBAMATE vs CERTICAN
CENOBAMATE vs CERTOLIZUMAB